EP1997622A1 - Fireproof glazing - Google Patents

Abstract

The transparent fire proof glazing comprises an intumescent layer (3) between glass sheets (1, 2). The intumescent layer is a layer of hydrated alkaline silicate in the preparation of which the silica (60 wt.%) is introduced in the form of an aqueous suspension of silica particles with an average grading of 50-130 nm, and has water content (35-43 wt.%). Molar ratio of silica to alkaline in the layer is 3.5-6. Adherence of the intumescent layer with the glass sheets is favored by applying adherence promoters on the glass sheets or by incorporating the promoters in the intumescent composition. The transparent fire proof glazing comprises an intumescent layer (3) between glass sheets (1, 2). The intumescent layer is a layer of hydrated alkaline silicate in the preparation of which the silica (60 wt.%) is introduced in the form of an aqueous suspension of silica particles with an average grading of 50-130 nm, and has water content (35-43 wt.%). Molar ratio of silica to alkaline in the layer is 3.5-6. Adherence of the intumescent layer with the glass sheets is favored by applying adherence promoters on the glass sheets or by incorporating the promoters in the intumescent composition. The dried intumescent sheet is separated from the support sheet. An independent claim is included for a process for preparing a transparent fire proof glazing.

Description

The present invention relates to fire-resistant glazing comprising at least one layer of a hydrated alkali silicate whose exposure to fire causes the formation of an opaque foam which opposes the transmission of radiation and maintains the glass sheets to which the layer or layers of alkali silicate are associated.

The use of hydrated alkali silicates in the manufacture of fireproof glazing is carried out in two distinct modes.

The first mode comprises the products in which the layer (s) of silicates are formed from commercial solutions of these silicates, solutions to which are added various additives which improve the properties and / or the conditions of use. Starting from these solutions, the layers are obtained by spreading the solution on a support and by drying more or less prolonged until a solid layer is obtained. The silicate layer thus formed, possibly directly on a glass sheet, is then included in a laminated assembly between two sheets of glass.

For this first family of products the conditions of preparation, and particularly those of drying are relatively restrictive.

The choice of the drying pathway from industrial alkali silicates also has consequences with regard to the mechanical properties of the glazings incorporating these silicate layers. The low water content chosen to avoid alteration in time of the transparency properties, does not allow to have very "plastic" layers. The consequence is a limitation of the so-called "soft impact" resistance, which resistance is necessary in certain applications, particularly in external glazing, and which must be compensated for by a particular structure, for example by association with laminated sheets comprising an interlayer. of a thermoplastic material, or more often by the addition of compounds that increase the plasticity of the intumescent layer. For plasticizing products, polyols, in particular glycols, are most often used. The presence of these is relatively important for the lowest moisture content. Thus for water contents of the order of 20 to 25% by weight it is usual to introduce about 15% by weight or more of ethylene glycol or glycerin. The presence of such amounts of organic products is not advantageous with respect to the fire behavior. They lead to carbonization and the release of unwanted fumes.

The second traditional mode relates to products in which a relatively high water content silicate solution is frozen by the addition of products referred to as "hardeners", "crosslinking agents" or otherwise. These qualifiers generically refer to products that promote the gelation of the silicate solution. They are carefully selected, so that after their addition to the silicate solution, the silicate solution cures spontaneously in a relatively short time, without the need for drying.

For these products, before gel formation, the solution with its additives is poured between two sheets of glass delimiting an enclosed space. A seal located at the periphery of the glass sheets tightly associates them and holds the solution during its gelation.

The absence of drying is a definite advantage with regard to the mode of production. The products in question obviously retain a relatively high water content. This content is chosen so that the silicate solution can not give rise to premature gelation making it impossible to use it later. The stability over time of these solutions is indeed a function of this water content.

Typically the compositions used without prior drying, have a water content of about 47-48% by weight. The publications on this subject do not propose a composition with a water content of less than 44%, because of the lower water content. led to a composition whose fluidity could not be guaranteed enough time ("pot life").

It should be noted that water tenure means that which can be determined by complete evaporation. This content does not take into account how the water is possibly in these "hydrated" silicate compositions.

The presence of this relatively abundant water can lead to a lack of cohesion of the glazing. Subject to shear forces in the plane of the glazing, the glass sheets, even at ordinary temperature are likely to play against each other.

The high water content can also produce a very irregular "foam", detrimental to the integrity of the fireproofed sheet. In order for these products to have the "mechanical" qualities required for the fire test, use is made of means that compensate for the insufficient properties of the intumescent layer. For example, instead of annealed glass sheets, tempered glass is used. This solution increases the cost of the products but above all requires the production to the final dimensions required, the subsequent cutting is not possible.

Moreover, high proportions of water in the intumescent layer require strengthening the edge protection to avoid alteration over time, consecutive for example to a progressive drying from these edges.

An object of the invention is to provide the formation of fireproof glazing comprising intumescent layers that can be formed without drying, and without these layers retain a water content such that it leads to deficiencies, particularly relating to fire resistance, indicated above.

An object of the invention is to provide the formation of glazing whose intumescent layer or layers offer a relatively high refractoriness.

Another object of the invention is notably to propose the formation of such glazings in the intumescent layers from which the water content remains sufficient to guarantee adequate plasticity.

Another object of the invention is to ensure that the water content does not lead to deterioration of the optical properties, in particular does not lead to the presence of a "haze".

The inventors have shown that it is possible to obtain fluid compositions of alkali silicates which harden without drying, and whose water content can be substantially less than those of analogous compositions of the prior art. Obtaining these properties, according to the invention, is related to the method of preparation of the composition. This preparation systematically comprises as silica-providing materials, at least in part, suspensions of colloidal silica particles whose particle size is very specific.

In practice, the inventors have demonstrated the relationship between the rheological behavior of the alkali silicate compositions and the silica particle dimensions used in these compositions. The methods of preparation of these silicate compositions are also part of the invention.

The traditional method of preparing the intumescent layers, with or without drying, involves the use of industrial alkali silicate solutions as the base compound. These solutions have characteristics that limit the possibilities of use. In particular they have relatively high water contents, and these levels are all the more important that the molar ratio SiO ₂ / M ₂ O is itself greater.

As an indication, the water content of commercial solutions of alkali silicates is of the order of 65% by weight for a molar ratio of 3.3, and of the order of 45% for a molar ratio of 2. These industrial solutions are adjusted to maintain adequate viscosity for their users. At the values indicated above, the viscosity is about 100mPa.s.

For fire-resistant glazing, larger molar ratios are preferable for improving refractoriness. It therefore appears that the alkaline silicates of commerce are not usable, or not usable as such for the preparation of intumescent compositions, especially when it is a product whose drying is to be avoided, the water contents being much too high .

In practice according to the invention, the intumescent layers produced and used in fireproof glazings advantageously have an SiO ₂ / M ₂ O molar ratio of between 3 and 8, and preferably between 3.5 and 6, and particularly preferably preferred between 3.5 and 5, and their water content is between 30 and 48% and preferably between 35 and 43%.

According to the mode of application leading to the glazing, namely either by casting between two sheets constituting a kind of container of the liquid composition, the hardening taking place between the sheets, or by applying the solution on a horizontal sheet, a second sheet Since the glass is subsequently applied to the intumescent layer when the curing is started or even completed, the water content may be more or less important.

The implementation between two sheets preferably requires a slightly higher water content to maintain a low viscosity which facilitates the eventual elimination of bubbles. Particularly preferably in this case the water content is 40 to 43% by weight. In the case where the solution is spread on the sheet in a horizontal position, the viscosity of the composition may be a little higher and consequently the water content is advantageously less, and is particularly preferably from 35 to 41%.

In any case, commercial solutions of alkali silicates can not be used as such. Given the significant differences between these compositions and those used for the formation of the layers according to the invention, it may be preferable to proceed to the preparation of the latter without using, even partially, the industrial solutions.

To prepare the compositions used, it is advantageous to start from suspensions of colloidal silica and alkaline hydroxide. The latter is either in the form of a solution or at least partly in the form of solid pellets to limit as much as possible the water content of the mixture. The concentrations of the hydroxide solutions can be relatively high. The weight content of metal oxides can reach 50% in the solutions. It can be 85% in the pellets. If the silica suspensions do not usually exceed 50% by weight of silica, the compositions obtained by reaction of these suspensions with the alkaline hydroxide may have a substantially lower water content than industrial silicates and this with molar ratios SiO ₂ / M ₂ O much higher. In addition, the reproducibility of the compositions and the regularity of the properties of the products obtained are all the better ensured by this method of preparation.

If nevertheless for reasons of economy, it is preferred to use at least partially industrial silicates, it remains necessary to modify them by a substantial supply of colloidal silica to achieve compositions having the desired molar ratios without having to eliminate a quantity excessive water.

In all cases, the preparation of the alkali silicate compositions used in the formation of the intumescent layers without drying passes through the use of colloidal silica suspensions. According to the invention, the proportion of silica originating from these suspensions of colloidal silica in the intumescent material is advantageously at least 50%, preferably at least 60%, and particularly preferably at least 70%. The silica present can come entirely from colloidal suspensions.

The inventors have found that the hardening of the alkali silicate solutions in which the use of silica suspension is involved, the composition being otherwise identical, depends at least partly on the size of the silica particles used.

In general, it has become apparent to the experiment that the increase in the size of the particles, within certain limits, makes it possible to delay the setting of the composition as a mass. As a result, compositions in which the size of the silica particles is increased, may have a reduced water content compared to the compositions of the prior art, while maintaining the fluidity required for a time sufficient for use under the usual conditions.

If the prior compositions usable did not allow to go below a water content of 44%, and in practice did not fall below 47-48%, the use according to the invention of silica having particles of dimensions as taught by the invention, can achieve much lower water content, up to 30% by weight, while retaining the necessary rheological properties.

The mechanisms that lead to these properties are not fully understood. They use complex phenomena associating the silica particles within the composition. The formation of more or less structured aggregates seems to depend on the immediate environment of the particles likely to bind to each other. The constituted network would be even more "tight", and therefore the composition less fluid, that the links are more numerous. At a constant amount of silica, the surface available for the formation of these bonds is larger the smaller the particles. In other words the formation of the network leading to the setting in mass of the composition is favored by the presence of small particles.

It goes without saying that the increase in particle size is limited. Beyond a certain dimension, the compositions no longer exhibit the required optical properties, and in particular transparency. Too large dimensions lead to a diffusion of light, or in the usual terms, to the formation of a haze.

In practice, the silica particles used for the formation of the alkali silicate compositions have an average diameter of not less than 40 nm and preferably not less than 50 nm. These particles also have average dimensions which do not exceed advantageously 150 nm and preferably not 130 nm. The particularly preferred average diameter is between 60 and 120 nm.

The particle sizes of the same silica suspension are ordinarily well homogeneous. A share of not less than 80% by weight of the particles is within ± 10% of the average diameter.

The dimensions of the silica particles in the suspensions used, appear well defined in the observation in electronic optics. The measurement of these dimensions, apart from the optical observation, can be made by electroacoustic examination (using for example an "acoustosizer" type of apparatus), by photon correlation spectroscopy (for example by using an apparatus type "Coulter Delsa 440SX"), or by centrifugation.

Depending on the method of preparation adopted, and depending on the desired water content in the final composition, once the mixture of constituents has been produced, it may be necessary to adjust the water content. For this, dehydration can be implemented. In any case, it is of course preferable to ensure that the mixture of the various constituents results in a composition whose water content is that of the composition of the final intumescent layer, or at least be as close as possible to that of -this. Advantageously, and to limit the possible dehydration operation, the water content in the composition as prepared is not greater than 50% by weight.

When dehydration is necessary, it is advantageously made by subjecting the product to evaporation under partial pressure. Dehydration in this case has the advantage of simultaneously leading to degassing of the product. This prevents the risk of bubble entrainment in the layer prepared from this composition.

Dehydration can be done at room temperature. A slightly higher temperature can accelerate the removal of water. However, this warming of the composition must remain very limited to avoid any risk of early en masse. In practice the temperature does not exceed 60 ° C.

After adjusting the water content, the composition may be stored for several hours or even days at room temperature prior to use. When the conditions of preparation, and in particular when the choice of silica particles is carried out according to the methods of the invention, the composition may be stored for at least 48 hours. If the preservation time has to be prolonged well beyond, it is preferable to avoid any risk of caking, to refrigerate the composition for example at about 4 ° C. At these temperatures the pot life can be greatly increased.

The intumescent layer is mainly composed of alkaline silicates and water. The silicates are those potassium, sodium and lithium. It is possible to have a mixture of these silicates, however such a mixture is not preferred because it leads to layers whose softening temperature is lowered.

Potassium silicates are preferred. They advantageously represent at least 60% by weight of all the silicates, and preferably at least 80%. In a particularly preferred manner, all the silicates used, with inevitable impurities, that is to say more than 95% by weight, consists of potassium silicate.

Apart from silicates and water, various additives may be introduced into the composition, in particular polyols, and in particular ethylene glycol or glycerol.

In the dried intumescent products of the prior art, the introduction of these polyols is intended in particular to compensate for the lack of plasticity of the products whose water content is very low (from 20 to 25%). The polyol content can then be up to 18-20% by weight in the layer formed. In the intumescent layers prepared according to the invention, when polyols are present, their content remains much lower. It is advantageously not greater than 10% by weight of the composition, and preferably not greater than 8%.

Preferred levels of glycols, especially ethylene glycol or glycerin, are between 2 and 6% by weight of the final layer.

Traditionally intumescent compositions also comprise other additives in small proportions. These are nitrogen products (urea, amines, etc.) or surfactants.

Advantageously, the compositions contain tetra-methyl ammonium hydroxide (TMAH) at a content which is not greater than 2% by weight.

The prepared solution is sufficiently stable at ordinary ambient temperature conditions. It can be stored for several hours, or even days if necessary by cooling, without the risk of formation of a gel. It is possible to use this stability to eliminate bubbles that may have appeared in the mixing of the mixture. The removal can take place simply by leaving the solution at rest or by any known technique such as the use of ultrasound or degassing under partial pressure, for example.

An object of the invention, as indicated above, is to provide an intumescent composition that does not require any drying to achieve curing. This peculiarity, apart from the gain it brings to the production of the glazing, also allows the formation of intumescent layers whose thickness is not limited. Previously this thickness took into account the length of the drying time. In practice this increasing time as the square of the thickness, to remain within industrially acceptable limits, the thickness of the dried layers did not usually exceed 2 mm. The use of hardening layers without drying makes it possible to produce much thicker layers.

In practice, for some glazings it may be useful to form layers according to the invention with a thickness of up to 8mm, or even 10mm or more.

The use of thick layers can lead to products substantially different from those usually available. For example, the fire resistance qualities that lead in traditional techniques to increasing the number of layers and simultaneously glass sheets that support them, can be replaced by thicker layers and a smaller number of glass sheets. In other words, it is possible in this way to reduce the thickness, weight and cost of glazing for the same final quality.

• la figure 1 est une vue schématique en perspective d'un vitrage anti-feu élémentaire selon l'invention
• la figure 2 est un diagramme d'un mode de production de la composition intumescente selon l'invention;
• la figure 3 est un diagramme d'un autre mode de production de la composition intumescente selon l'invention ;
• la figure 4 est un diagramme illustrant deux modes de formation de vitrages selon l'invention.

The production of the glazings according to the invention is shown schematically in the appended figures in which:

• the figure 1 is a schematic perspective view of an elementary fire-resistant glazing according to the invention
• the figure 2 is a diagram of a mode of production of the intumescent composition according to the invention;
• the figure 3 is a diagram of another embodiment of the intumescent composition according to the invention;
• the figure 4 is a diagram illustrating two modes of forming glazing according to the invention.

The basic element of transparent fireproof glazing systematically consists of an intumescent layer 3, sandwiched between two sheets of glass 1 and 2. The glass sheets are represented as monolithic or, if appropriate, constituted by a laminated assembly including an interlayer sheet for example polyvinyl butyral type (PVB).

On the basis of this element the commercial fire-resistant glazing is developed in particular by combining in the same set several intumescent layers and several sheets of glass, identical or different depending on the intended use. In practice, the multiplication of the layers is intended in particular to increase the fire resistance characteristics, the multiple intumescent layers adding their effects. Such assemblies are advantageously replaced by others in which the layers are thicker, the formation mode without drying being suitable for the reasons indicated above for the formation of thick layers.

The figure 2 schematically shows a mode of preparation of the intumescent composition. In the preferred embodiment, the silicate composition is formed from an alkaline hydroxide mixture MOH and a suspension of SiO ₂ silica particles. In addition to these basic constituents, additives, in particular glycols, surfactants, etc., may be added.

The mixing is carried out to achieve the appropriate compositions according to the invention namely a water content (excluding potential organic additives) as low as possible and close to 50% or less, with a relatively high molar ratio as indicated above. The mixing is carried out with stirring to homogenize the composition as shown.

The composition 4 is degassed to remove any bubbles present after this mixture. It is optionally dehydrated to adjust the water content.

The intumescent composition is stable at ordinary temperature. It is even more conserved at about 4 ° C.

The figure 3 illustrates the variant in which a part of the silica of the composition comes from industrial silicate solution. As previously, at least 50% of the silica consists of colloidal silica meeting the stated characteristics. The composition obtained 6 usually has a higher water content than in the previous case. Dehydration should be systematically performed.

The figure 4 shows two ways of using prepared intumescent compositions.

To the figure 4a the liquid composition is applied to a glass sheet 5 kept horizontal. The liquid composition layer 7 cures without drying on this sheet. A second glass sheet 8 covers the layer 7 during or after curing.

The setting in mass of the intumescent composition occurs spontaneously. However, it is advantageously accelerated by heating at moderate temperature. This heating is preferably performed at less than 80 ° C.

To improve the adhesion of the intumescent layer to the glass sheet it is also possible to apply thereon, or to introduce into the composition, compounds promoting this adhesion. They are, for example, silanes optionally comprising functional groups such as amino-silanes.

The superposition operation of the glass sheets and the intumescent layers optionally comprises several intumescent layers and as many additional glass sheets. These intumescent layers and glass sheets are identical or different depending on the intended applications.

The final assembly is advantageously carried out by calendering between rolls as indicated in 9. It is also possible to proceed to an autoclave. The temperature of the autoclave is associated with the pressure used. As an indication under 13 relative atmospheres, the temperature does not exceed 130 ° C.

In the manner presented to figure 4b the intumescent composition is poured into the space delimited by two sheets of glass 10 and 11 joined at their edges by a bead of material 12 which makes this space tight. As before, the composition cures without drying between the glass sheets.

The application of the composition may also be carried out on a continuous support, the layer then being recovered in the form of a ribbon The silicate solution prepared as above is poured onto the horizontal conveyor, preferably made of a polymer material The conveyor thus coated advantageously passes through an oven accelerating hardening The hardened intumescent sheet is separated from the conveyor belt and possibly wound on itself To prevent the turns from sticking to each other the sheet can be interleaved with an interleaf during storage. The intumescent sheet thus prepared can be subsequently assembled with glass sheets as before.

The impact of the silica particle size of the colloidal suspensions on the setting time and on the optical quality of the compositions is the subject of the following tests.

Two types of silica suspensions are used which each have the same silica content of 50% by weight of the suspension. One of the suspensions comprises particles whose average diameter is 30 nm, the other of particles of average diameter 70 nm, in other words whose specific surface is less than 4 times that of the first suspension.

The mixture formed is 50% by weight of the silica suspension and 50% by weight of 50% KOH solution. The mixture, if any, of the amount of ethylene glycol (EG) or glycerine (G), and of TMHA (T) is degassed and slightly dehydrated until the water contents indicated in the table are obtained. next.

The mixture is observed for its optical qualities and for maintaining its fluidity. The viscosity limit that is set as sufficient to allow the use of the composition ("pot life") is 100mPa.s. Apparent composition Pot life at 20 ° C R _m EG BOY WUT T Water Particle diameter of the SiO ₂ vector SiO ₂ / K ₂ O % % % % 30nm 70nm 3.8 4 0 1 50 <4h > 48h 4 0 1 48 <4h > 40h 4 0 1 46 <4h > 36h 4 0 1 40 not transparent > 8h 4 0 1 38 not transparent > 8h 4.6 4 0 1 38 not transparent > 8h 0 7 1 38 not transparent > 8h

It is found that in all cases, the compositions comprising silica whose particles are 70nm in diameter has a shelf life in the liquid state much higher than that of similar compositions in which the silica particles are only 30nm. In addition, the solutions with a low water content (38% by weight) for the compositions according to the invention remain very transparent whereas that of the comparative examples is no longer transparent.

Claims (17)

Transparent fire-resistant glazing comprising at least one layer of intumescent material comprised between sheets of glass, wherein the intumescent layer is a hydrated alkali silicate layer in which the silica is at least partially introduced as an aqueous suspension of particles silica whose average particle size is greater than 40 nm and preferably greater than 50 nm. Fire-resistant glazing according to claim 1, in the preparation of the intumescent layer of which at least a portion of the silica is introduced in the form of an aqueous suspension of silica particles whose average particle size is less than 150 nm and preferably less than 130 nm. . Glazing according to one of the preceding claims, in which the proportion of added silica having the indicated particle size characteristics, with respect to the whole of the silica present in the intumescent layer, is at least 50% by weight and preferably from less than 60% by weight. Glazing according to one of the preceding claims wherein the intumescent layer has a water content of between 30 and 48% by weight, and preferably between 35 and 43%. Glazing according to one of the preceding claims wherein in the intumescent layer, the molar ratio of silica to alkali of the intumescent layer is between 3 and 8, and preferably between 3.5 and 6. Glazing according to one of the preceding claims wherein in the intumescent layer, the alkaline component is sodium, potassium, lithium or a mixture of several of them. Glazing according to claim 6 wherein the alkaline component consists of at least 60% by weight of potassium and preferably at least 80%. Glazing according to claim 7 wherein the totality of the alkaline component is potassium. Glazing according to one of the preceding claims, wherein the intumescent layer also contains polyols in a proportion of less than 10% by weight, and preferably less than 8%. Glazing according to one of the preceding claims wherein the adhesion of the intumescent layer to the glass sheets with which it is in contact is to promote by application of adhesion promoters on these sheets or by incorporation of these promoters in the intumescent composition. Glazing according to claim 10 wherein the adhesion promoters are silanes or silanes with amino-silane functional groups. Process for the preparation of fireproof glazing according to one of the preceding claims, comprising at least one intumescent layer formed from: or from an alkaline hydroxide solution to which an aqueous silica suspension is added, the particles of which have the appropriate particle size; or an alkali silicate solution to which is added a quantity of aqueous suspension of silica, the particles of which have the appropriate particle size; - Or by a set comprising partly an alkali silicate solution, partly an alkali hydroxide solution, to which is added the silica suspension whose particles have the appropriate particle size. The process of claim 12 wherein the hydrated alkali silicate composition in which all components are joined is applied to a glass sheet horizontal according to the desired thickness, the solution being left to mass, a second glass sheet being applied to the hardened layer, the assembly being assembled by calendering and / or passage to the oven. A process according to claim 12 wherein the hydrated alkali silicate composition is poured into the space between two glass sheets at the periphery of which is a sealed bead, the composition curing in this space. A process according to claim 13 or claim 14 wherein the setting of the intumescent solution is accelerated by heating to a temperature not exceeding 80 ° C. A process according to claim 13 or claim 14, wherein the setting of the solution is achieved by autoclaving at a temperature not exceeding 130 ° C under a pressure of 13 atmospheres. Glazing according to one of claims 12 or 13 wherein the dried intumescent layer is detached from the carrier sheet used during drying, the intumescent sheet being assembled with at least two sheets of glass.

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